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Cardiac and skeletal muscle disorders caused by mutations in the intracellular Ca(2+) release channels
Here we review the current knowledge about the mutations of the gene encoding the cardiac ryanodine receptor (RyR2) that cause cardiac arrhythmias. Similarities between the mutations identified in the RyR2 gene and those found in the gene RyR1 that cause malignant hyperthermia and central core disea...
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| 主要な著者: | , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Society for Clinical Investigation
2005
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1180555/ https://ncbi.nlm.nih.gov/pubmed/16075044 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI25664 |
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